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Cellosaurus FAMRCi011-B (CVCL_B5H5)

[Text version]
Cell line name FAMRCi011-B
Synonyms ARVC51b
Accession CVCL_B5H5
Resource Identification Initiative To cite this cell line use: FAMRCi011-B (RRID:CVCL_B5H5)
Comments From: Federal Almazov North-West Medical Research Centre; St. Petersburg; Russia.
Population: Caucasian.
Omics: Array-based CGH.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:3756; FLNC; Simple; p.Arg1267Gln (c.3800G>A); ClinVar=VCV000539409; Zygosity=Heterozygous (hPSCreg=FAMRCi011-B).
Disease Familial restrictive cardiomyopathy 5 (NCIt: C183309)
Familial isolated restrictive cardiomyopathy (ORDO: Orphanet_75249)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_B5H4 ! FAMRCi011-A
Sex of cell Male
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; FAMRCi011-B
Biological sample resources BioSamples; SAMEA9687269
Encyclopedic resources Wikidata; Q110432801
Entry history
Entry creation16-Dec-2021
Last entry update19-Dec-2024
Version number5